US2023345983A1PendingUtilityA1
Flavour compositions for improving taste impressions
Est. expiryMay 4, 2040(~13.8 yrs left)· nominal 20-yr term from priority
A23L 27/215A23L 27/22A23L 27/204A23L 27/2028A23L 27/2022A23L 27/2054A23J 3/14A23L 27/88A23L 27/84A23J 3/227A23L 27/2024A23L 27/26
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Claims
Abstract
The present invention relates to new flavour compositions, a method for producing such flavour compositions, the use of such flavour compositions for enhancing and/or imparting desired taste impressions and/or for reducing and/or masking undesired taste impressions, as well as to a product or semi-finished product comprising such a flavour composition. Furthermore, the present invention relates to the use of a sugar composition in the preparation of such a flavour composition.
Claims
exact text as granted — not AI-modified1 . A flavour composition comprising:
(a) Tyrosine, Phenylalanine, Tryptophan, and Glutamic acid,
wherein the Tyrosine and the Glutamic acid are in a weight ratio of 0.5 to 1,
the Phenylalanine and the Glutamic acid are in a weight ratio of 0.5 to 1, and
the Tryptophan and the Glutamic acid is are in a weight ratio of 0.05 to 0.3.
2 . The flavour composition of claim 1 , further comprising:
(b) one or more compounds selected from aldehydes, fatty acids, phenols, and ketones.
3 . The flavour composition of claim 2 , wherein the one or more compounds of (b) comprise
2-methylbutanal and isovaleraldehyde, 2-methylbutanal and 5,2,2-transmethylphenyl hexenal, and/or 2-methylbutanal and isobutyraldehyde.
4 . The flavour composition of claim 1 , further comprising:
(c) one or more pyrazines.
5 . The flavour composition of claim 4 , wherein the one or more pyrazines of (c) are selected from:
2,5-dimethylpyrazine and one or both of 2,5-methylethylpyrazine and 2,6-methylethylpyrazine, and 2,5-dimethylpyrazine and 2,3,5-trimethylpyrazine.
6 . The flavour composition of claim 1 , further comprising: d) one, two, three or more substance(s)
(d) one or more substances selected from edible acids, sugars, ribonucleotides, nucleosides, and minerals.
7 . The flavour composition of claim 1 , producible by a method comprising:
(a) enzymatic degradation of proteins to obtain a mixture comprising amino acids or providing a mixture comprising amino acids; (b) optionally, adding carbohydrates to the mixture; (c) heating the mixture obtained of (a) or (b) to apply a Maillard reaction; and (d) optionally, drying the mixture.
8 . The flavour composition of claim 7 , wherein the proteins are vegetable proteins, the carbohydrates are obtained from cereals, and the mixture of (a) or (b) is heated to a temperature of 130° C. to 140° C.
9 . A method for producing a flavour composition of claim 1 comprising:
(a) enzymatic degradation of vegetable proteins to obtain a mixture comprising amino acids or providing a mixture comprising amino acids;
(b) optionally, adding carbohydrates to the mixture;
c) heating the mixture of (a) or (b) to apply a Maillard reaction; and
d) optionally, drying the mixture.
10 . A method for improving a desired taste impression of a preparation comprising adding the flavour composition of claim 1 to the preparation and improving the desired taste impression of the preparation.
11 . A method for reducing or masking an undesired taste impression of a preparation comprising adding the flavour composition of claim 1 to the preparation and reducing or masking the undesired taste impression.
12 . A preparation comprising 0.001 to 70 wt.-% of the flavor composition of claim 1 , relative to a total weight of the preparation. in the preparation or semi-finished product is in a range of from 0.001 to 70 wt.-%, preferably in a range of from 0.005 to 50 wt.-%, further preferably in a range of from 0.01 to 10 wt.-%.
13 . The preparation of claim 12 being a protein-based or protein-enriched preparation.
14 . The method of claim 9 comprising:
(a) enzymatic degradation of vegetable proteins to obtain a mixture comprising amino acids;
(b) adding carbohydrates to the mixture, wherein the carbohydrates are obtained from cereals and comprise rhamnose, arabinose, galactose and/or xylose;
(c) heating the mixture obtained of (a) or (b) to a temperature of 130° C. to 140° C. to apply a Maillard reaction; and
(d) drying the mixture.
15 . The method of claim 14 , wherein the carbohydrates of (b) are added in an amount such that:
rhamnose is in a range of from 0.05 to 1.5 wt.-%, arabinose is in a range of from 1 to 10 wt.-%, galactose is in a range of from 0.1 to 5 wt.-%, and/or xylose is in a range of from 0.1 to 5 wt.-%, relative to a dry weight of the mixture before the heating of (c).
16 . The flavor composition of claim 1 , further comprising:
(b) one or more compounds selected from 2,2-transphenylbutenal, caprylic acid, 2-heptanone, 2-methylbutanal, 5,2,2-transmethylphenyl hexenal, caprinic acid, isobutyraldehyde, isovaleraldehyde, phenylacetaldehyde, vinyl guaiacol, 3-methyl thiopropanal and benzaldehyde.
17 . The flavor composition of claim 1 , further comprising:
(b) 2-methylbutanal.
18 . The flavor composition of claim 4 , wherein the one or more pyrazines are selected from 2,3-methylisobutylpyrazine, 2,3-dimethylpyrazine, 2,3,5-dimethylethylpyrazine, 2,3,6-dimethylethylpyrazine, 2,3,5-trimethylpyrazine, 2,5-dimethylpyrazine, 2,5-methylethylpyrazine, 2,6-methylethylpyrazine, 2-methylpyrazine, 2,6-dimethylpyrazine and 2-ethylpyrazine.
19 . The flavour composition of claim 18 comprising 2,5-dimethylpyrazine.
20 . The flavour composition of claim 1 in the form of a powder.Join the waitlist — get patent alerts
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